Polymerase Chain Reaction (PCR) and Its Applications

1. Polymerase Chain Reaction (PCR) and Its Applications by Ayaz Najafov

2. What is PCR? PCR is an exponentially progressing synthesis of the defined target DNA sequences in vitro. It was invented in 1983 by Dr. Kary Mullis, for which he received the Nobel Prize in Chemistry in 1993.

3. What is PCR? : Why “Polymerase”? It is called “polymerase” because the only enzyme used in this reaction is DNA polymerase.

4. What is PCR? : Why “Chain”? It is called “chain” because the products of the first reaction become substrates of the following one, and so on.

5. What is PCR? : The “Reaction” Components 1) Target DNA - contains the sequence to be amplified. 2) Pair of Primers - oligonucleotides that define the sequence to be amplified. 3) dNTPs - deoxynucleotidetriphosphates: DNA building blocks. 4) Thermostable DNA Polymerase - enzyme that catalyzes the reaction 5) Mg++ ions - cofactor of the enzyme 6) Buffer solution – maintains pH and ionic strength of the reaction solution suitable for the activity of the enzyme

6. The Reaction PCR tube THERMOCYCLER

7. Denature (heat to 95oC) Lower temperature to 56oC Anneal with primers Increase temperature to 72oC DNA polymerase + dNTPs

11. Classification of organisms Genotyping Molecular archaeology Mutagenesis Mutation detection Sequencing Cancer research Detection of pathogens DNA fingerprinting Drug discovery Genetic matching Genetic engineering Pre-natal diagnosis Applications of PCR

12. Applications of PCR Basic Research Applied Research • Mutation screening • Drug discovery • Classification of organisms • Genotyping • Molecular Archaeology • Molecular Epidemiology • Molecular Ecology • Bioinformatics • Genomic cloning • Site-directed mutagenesis • Gene expression studies • Genetic matching • Detection of pathogens • Pre-natal diagnosis • DNA fingerprinting • Gene therapy

13. Applications of PCR Molecular Identification Sequencing Genetic Engineering • Bioinformatics • Genomic cloning • Human Genome Project • Site-directed mutagenesis • Gene expression studies • Molecular Archaeology • Molecular Epidemiology • Molecular Ecology • DNA fingerprinting • Classification of organisms • Genotyping • Pre-natal diagnosis • Mutation screening • Drug discovery • Genetic matching • Detection of pathogens

14. MOLECULARIDENTIFICATION:

16. Molecular Identification: Detection of Unknown Mutations

17. SSCP gels:“shifts” representing a mutation in the amplified DNA fragment

18. Insufficient data Molecular Identification: Classification of Organisms 1) Relating to each other 2) Similarities 3) Differences * Fossils * Trace amounts * Small organisms ! DNA !

20. Rademaker et al. 2001

21. Molecular Identification: Detection Of Pathogens

22. Molecular Identification: Detection Of Pathogens Sensitivity of detection of PCR-amplified M. tuberculosis DNA. (Kaul et al.1994)

23. Sensitivity of detection of PCR-amplified M. tuberculosis DNA. (Kaul et al.1994)

24. Molecular Identification: Genotyping by STR markers

25. 644 bp 440 bp 204 bp Molecular Identification: Prenatal Diagnosis • Chorionic Villus • Amniotic Fluid Molecular analysis of a family with an autosomal recessive disease.

26. SEQUENCING Nucleotides (dNTP) are modified (dideoxynucleotides = ddNTP) NO polymerisation after a dideoxynucleotide! Fragments of DNA differing only by one nucleotide are generated radioactive Nucleotides are either or fluorescent

28. Sequencing: Classical Sequencing Gel

29. Sequencing: Reading Classical Sequencing Gels

30. Sequencing:

31. Summary blood, chorionic villus, amniotic fluid, semen, hair root, saliva 68,719,476,736 copies Gel Analysis, Restriction Digestion, Sequencing

32. Conclusion The speed and ease of use, sensitivity, specificity and robustness of PCR has revolutionised molecular biology and made PCR the most widely used and powerful technique with great spectrum of research and diagnostic applications.